Cervarix – Cervical Cancer VaccineGSK's Cervarix® is a prophylactic vaccine against human papilloma virus (HPV) types 16 and 18. It is being developed for the prevention of precancerous cervical lesions (high-grade cervical intraepithelial neoplasia: CIN grades 2 and 3) and cervical cancer associated with HPV types 16 and 18. Already licensed in Europe for use in females aged 10–25 years, the company had hoped for similar success in the US, where it filed for regulatory approval in March in 2007. However, at the end of 2007, the US FDA issued a 'complete response letter' detailing a series of questions that must be addressed before it will clear Cervarix for launch. Analysts have speculated that this could result in significant delays to Cervarix's US debut and allow Merck & Co's competitor vaccine Gardasil® , which is already on the market, to become more entrenched. TARGETING HPV IN CERVICAL CANCER PREVENTION HPV is a common sexually transmitted disease that has been implicated in the development of precancerous cervical lesions and cervical cancer. Around 100 types of HPV have been identified to date, of which types 16 and 18 are believed to be responsible for more than 70% of cervical cancers that occur in Europe. Most of the remaining 30% of cases of cervical cancer are thought to be associated with other high-risk types of HPV. "Cervarix clinical trials have shown vaccination to be 100% effective in preventing cervical lesions due to HPV types 16 and 18 in women aged 15–25 years"
Vaccines developed against HPV types 16 and 18 are designed to prevent the acquisition of HPV infection in at-risk females, therefore providing protection against the development of precancerous cervical lesions that may arise from persistent HPV infection and subsequently lead to cervical cancer. Since many sexually active women contract HPV infection during their lifetime, prophylactic vaccination needs to be given before females become sexually active. Current immunisation schemes are targeted at children and adolescents who have not yet been exposed to the HPV virus through sexual activity. MATHEMATICAL MODELLING POINTS TO EFFECTIVE PREVENTION Since it can take many years for cervical cancer to develop, any benefits from prophylactic vaccination will not be seen for a considerable time. However, the number of cases of precancerous changes in the cervix (CIN) can be expected to fall much more quickly. Evidence from the Cervarix clinical trials programme has shown vaccination with Cervarix to be 100% effective in preventing cervical lesions due to HPV types 16 and 18 in women aged 15–25 years, when followed over a 5.5 year period. Evidence from mathematical modelling, designed to assess the lifetime clinical benefit of vaccination in cervical cancer prevention, also suggests that vaccination against HPV types 16 and 18 can make a major contribution to reducing the number of cases of cervical cancer as well as deaths from cervical cancer. With 100% coverage of all 12-year old girls in the US, the model predicted that 70% of cervical cancer cases could be prevented. Even 70% vaccine coverage would achieve a 50% reduction. CERVARIX GOES HEAD-TO-HEAD WITH GARDASIL Although Merck & Co's Gardasil has beaten Cervarix to the US market, GSK is hopeful that results of an ongoing head-to-head trial of the two vaccines will show Cervarix to be the superior of the two vaccines. The randomised, observer-blind study, involving over 1,000 women, is designed to compare the immunogenicity of the two vaccines in young women aged 18–26 years (primary endpoint) as well as in those aged 27–35 and 36–45 years (secondary endpoints). "With 100% coverage of all 12-year old girls in the US, it is predicted that 70% of cervical cancer cases could be prevented."
Cervarix is formulated with the proprietary adjuvant system AS04, which both enhances the immune response and increases the duration of protection against cancer-causing virus types; properties which the company believes may confer benefits over its rival. In studies, the ASO4 formulation of Cervarix induced higher antibody levels and a more sustained immunological response when compared with a conventionally formulated vaccine with aluminium hydroxide adjuvant alone. MARKETING COMMENTARY After breast cancer, cervical cancer is the second leading cause of cancer in women under 45 years of age. Worldwide, over 270,000 women die from cervical cancer each year. While cervical screening has done much to improve early detection and outcome, a vaccine to prevent HPV infection may help to prevent many such cancers developing in the first place. Currently, GSK's Cervarix competes with Merck's Gardasil in most major markets around the world, with the exception of the US, where Gardasil still remains unchallenged.
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![]() Persistent infection with oncogenic types of human papilloma virus, such as types 16 and 18, can lead to the development of cervical cancer. | |
![]() Cervical cell abnormalities are classified as CIN 1-3. CIN 1 describes mild dysplasia, in which the cells often revert to a normal histological pattern. | ||
![]() In its early stages, cervical cancer is usually asymptomatic. Cervical cancer screening is important in detecting potentially pre-cancerous lesions. | ||
![]() Staging is important in determining the extent and spread of a cancer and the type of treatment likely to be most effective. | ||
![]() In the UK, GSK markets over 25 prophylactic vaccines for the prevention of serious infectious diseases. Cervarix is one of its most recent additions to the list. |
